About: Galbonolides A and B--two non-glycosidic antifungal macrolides

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scientific article published on 01 December 1986

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1986 (uk) article scientifique publié en 1986 (fr) im Dezember 1986 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1986 (ast) scientific article published on 01 December 1986 (en)
publication date	wds:Q69752528-D06A543D-7207-4C85-BE26-6AC001157267
publication date	1986-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q69752528-304D76F6-A85F-44B3-B6AB-2F0A6848BEEE wds:Q69752528-A8D7007F-DE7D-4C4A-8631-A7ED59A814A5 wds:Q69752528-E4B72DDE-9D30-447B-AF4E-0E7DFAB09421
cites work	Rustmicin, a new macrolide antibiotic active against wheat stem rust fungus Metabolic products of microorganisms. 166. Optimization of the desferri-ferricrocin production by Aspergillus viridi-nutans Ducker & Thrower (author's transl) Neorustmicin A, a new macrolide antibiotic active against wheat stem rust fungus
access restriction status	wds:Q69752528-03930A4E-7D46-43F0-BF2B-7B7BB161E2EF
access restriction status	open access
author name string	wds:Q69752528-6CBE7861-5773-4DDD-A8CF-AAB79B2E2A03 wds:Q69752528-ABE0DC70-9294-4213-A68C-6F484F483B9D wds:Q69752528-DD0C2F87-2630-4AA9-AAA2-1F2B3DD6E912 wds:Q69752528-E13B0EFA-B8B5-4E42-B9B9-953D8AB9D9A7
author name string	H Zähner U Fauth H Achenbach A Mühlenfeld
rdfs:label	Galbonolides A and B--two non-glycosidic antifungal macrolides (en) Galbonolides A and B--two non-glycosidic antifungal macrolides (nl)
skos:prefLabel	Galbonolides A and B--two non-glycosidic antifungal macrolides (en) Galbonolides A and B--two non-glycosidic antifungal macrolides (nl)
name	Galbonolides A and B--two non-glycosidic antifungal macrolides (en) Galbonolides A and B--two non-glycosidic antifungal macrolides (nl)
title	wds:Q69752528-77012C36-2F21-4EBC-9013-0DD904024807
title	Galbonolides A and B--two non-glycosidic antifungal macrolides (en)
page(s)	wds:Q69752528-0492F4B8-2F35-47F7-9596-881C783CE39F
page(s)	1760-1764
instance of	wds:Q69752528-7CF91D9C-877B-4602-B016-B551D04FD436
instance of	scholarly article
main subject	wds:Q69752528-1257616F-B9D7-4754-BA82-A74F1AA8BB63 wds:Q69752528-29B8496F-6D53-4E76-8756-41DDB34C4B36
main subject	Streptomyces galbus (3R,5S,7Z,9S,12Z,14S)-14-ethyl-5-hydroxy-5-(hydroxymethyl)-3,7,9,13-tetramethyl-11-methylidene-1-oxacyclotetradeca-7,12-diene-2,4-dione
PubMed ID	wds:Q69752528-320C00DA-DEA1-4FE8-B14F-5D0751B7EC24
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3818448
PubMed ID	3818448
published in	wds:Q69752528-928901AF-7C26-4184-A35A-93BAF81C51B7
full work available at URL	wds:Q69752528-2682519C-0562-405F-A476-A17170F1A6E8
published in	The Journal of Antibiotics
full work available at URL	https://www.jstage.jst.go.jp/article/antibiotics1968/39/12/39_12_1760/_pdf
issue	wds:Q69752528-6A56A4AC-0AB5-49CF-B044-7E3D4C4E2E1A
volume	wds:Q69752528-09DA61E4-D611-403C-9551-0E3E8D7DC63A
issue	12
volume	39
DOI	wds:Q69752528-305E0128-2987-45B7-9CE7-1D02F6F1476E
DOI	http://dx.doi.org/10.7164/ANTIBIOTICS.39.1760
DOI	10.7164/ANTIBIOTICS.39.1760
online access status	wds:Q69752528-07A7EC1D-FF0B-491B-BFA3-967C88254160
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69752528
is cites work of	Comprehensive investigation of marine Actinobacteria associated with the sponge Halichondria panicea Microbial natural products as a source of antifungals Inhibition of fungal sphingolipid biosynthesis by rustmicin, galbonolide B and their new 21-hydroxy analogs Rustmicin, a potent antifungal agent, inhibits sphingolipid synthesis at inositol phosphoceramide synthase Taxonomy, Physiology, and Natural Products of Actinobacteria The role of 1,3-dithianes in natural product synthesis Inhibition of inositol phosphorylceramide synthase by the cyclic peptide aureobasidin A. Chemical tools to investigate sphingolipid metabolism and functions. The methoxymalonyl-acyl carrier protein biosynthesis locus and the nearby gene with the beta-ketoacyl synthase domain are involved in the biosynthesis of galbonolides in Streptomyces galbus, but these loci are separate from the modular polyketide sy Natural products as antifungal agents against clinically relevant pathogens Synthesis and antifungal activity of novel 14-membered benzomacrolides, as galbonolide analogues Yeast sphingolipid bypass mutants as indicators of antifungal agents selectively targeting sphingolipid synthesis Agroactive compounds of microbial origin Antimicrobial activities of Streptomyces pulcher, S. canescens and S. citreofluorescens against fungal and bacterial pathogens of tomato in vitro. Heterologous expression of galbonolide biosynthetic genes in Streptomyces coelicolor Sch 37137, a novel antifungal compound produced by a Micromonospora sp. Taxonomy, fermentation, isolation, structure and biological properties. A single module type I polyketide synthase directs de novo macrolactone biogenesis during galbonolide biosynthesis in Streptomyces galbus Separation and Purification of Macrolides Using the Ito Multi-Layered Horizontal Coil Planet Centrifuge Synthesis of a key intermediate of novel galbonolide analogues via efficient construction of a conjugated diene system Beneficial Endophytic Bacteria-Serendipita indica Interaction for Crop Enhancement and Resistance to Phytopathogens Fermentation studies of rustmicin production by a Micromonospora sp The galbonolides. Novel, powerful antifungal macrolides from Streptomyces galbus ssp. eurythermus A total synthesis of galbonolide B. Novel galbonolide derivatives as IPC synthase inhibitors: design, synthesis and in vitro antifungal activities [Metabolic products of microorganisms. 35. Asperdurin, a new antimycotic phthalide from Aspergillus duricaulis] In vitro reconstitution of a PKS pathway for the biosynthesis of galbonolides in Streptomyces sp. LZ35 Model studies for the synthesis of galbonolide B
is cites work of	wds:Q35105782-EEF61FCD-7494-4849-897A-87AF8C0E08C8 wds:Q44717716-E011A7A5-F1DD-4582-9888-DB07237BFC31 wds:Q44512414-1410DEC5-1C78-4A61-9861-25E4579AFE87 wds:Q40788565-78FCF2A8-2C0A-4977-8FBF-BC313AC2485A wds:Q42956211-FA15A9C9-902E-4CC0-95C5-497C82120147 wds:Q80438214-E2D869DB-66CE-4FFF-A4D3-12884E3CEB45 wds:Q92538206-45BB8204-29B5-453D-9A2A-2CE1E6D5635C wds:Q27938050-47007337-5A50-4FA2-8E9B-AA66133F011C wds:Q44698633-883C1176-6D17-4140-B215-E8467D56798D wds:Q86860410-84C4A90A-913A-4FBF-8AC2-149E08E15DDA wds:Q33876759-33F47AD3-9A22-43C8-8D20-2A11AC52E96A wds:Q38985975-CBF228FE-68F2-47AF-BF22-594243651A04 wds:Q46933979-4ABC52A8-C140-43A0-BE6C-8EC97473A2BD wds:Q45167698-9B0BD3BB-54E7-4AB0-A6C1-94468DF37817 wds:Q42538193-81BB3210-DC24-495C-8876-E4C7D4F35679

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